Allele Registry

Canonical Allele Identifier: PA356661

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000203960

RCV000562884

RCV003401108

ClinVar Variation:

220389

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Val427Ile	CA348239 NM_001127500.3:c.1279G>A